Fortrea

Job Overview:The Principal Strategy & Planning Specialist supports CPS clinical development strategy and external site partnerships by leveraging site capabilities feasibility data and key performance metrics. It collaborates closely with commercial and operational teams to provide st

Job Overview:The Principal Strategy & Planning Specialist supports CPS clinical development strategy and external site partnerships by leveraging site capabilities feasibility data and key performance metrics. It collaborates closely with commercial and operational teams to provide st

The QA Lead Manager is responsible for overseeing Quality Issue Management ensuring GCP compliance and providing expert QA support across clinical development teams. This role partners closely with crossfunctional stakeholders to investigate quality issues drive effective CAPA develop

The QA Lead Manager is responsible for overseeing Quality Issue Management ensuring GCP compliance and providing expert QA support across clinical development teams. This role partners closely with crossfunctional stakeholders to investigate quality issues drive effective CAPA develop

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Maintains an understanding of applicable r

Job Overview:Responsible for performing TMF review of electronic Trial Master Files (eTMF) Trial Country and Site artifacts for clinical studies in support of sponsors services contracts and internal business needs.Summary of Responsibilities:Maintains an understanding of applicable r

We are currently seeking an experienced Global Start Up Project Manager with 3 years of SUPM experience to join our team! Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and

We are currently seeking an experienced Global Start Up Project Manager with 3 years of SUPM experience to join our team! Job Overview:Accountable for execution and oversight of local operational clinical trial activities and has ownership oversight and impact on local regulatory and

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Summary of Responsibilities:Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc. (Language: French)Receive information record and report Adverse Drug Reaction in timelines (according to the regula

Summary of Responsibilities:Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call email fax etc. (Language: French)Receive information record and report Adverse Drug Reaction in timelines (according to the regula

Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Job Overview:Manage and develop clinical operations team consisting of Clinical Research Associates. Contribute to and oversee resource planning and assignments. Provide monitoring oversight to ensure all activities are conducted to the highest possible quality and in accordance with

Job Overview:As a Workday Extend Developer at Fortrea you will be responsible for designing developing and implementing custom applications and integrations within the Workday platform. You will work closely with cross-functional teams to understand business requirements develop solut

Job Overview:As a Workday Extend Developer at Fortrea you will be responsible for designing developing and implementing custom applications and integrations within the Workday platform. You will work closely with cross-functional teams to understand business requirements develop solut

Job Overview:Location: Warsaw (hybrid role)We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to

Job Overview:Location: Warsaw (hybrid role)We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Job Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study to ensure EC/IRB/Third body/Regulatory Authority and any other local applications

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

The Senior Site Navigator is responsible for coordinating and delivering site-level start-up activities for clinical studies acting as the primary point of contact for investigative sites throughout the study. The role ensures timely site activation regulatory compliance and effective

The Senior Site Navigator is responsible for coordinating and delivering site-level start-up activities for clinical studies acting as the primary point of contact for investigative sites throughout the study. The role ensures timely site activation regulatory compliance and effective

We are looking for a clinical operations professional to join our team as a Site Navigator II with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

We are looking for a clinical operations professional to join our team as a Site Navigator II with a significant Start-Up experience. This is an excellent role for someone looking to grow their career in clinical research within a global CRO environment.Summary of Responsibilities:Act

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all asp

Job Overview:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi

Job Overview:The Senior Clinical Trial Administrator (Sr. CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Sr. CTA shall reflect their experience and level of contribution whi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point of contact for investigative sites th

Job Overview:The Learning Specialist supports and facilitates learning and development activities. The role manages and maintains training facilities and resources coordinating event logistics for face-to-face training events providing and/or coordinating on-site and/or remote support

Job Overview:The Learning Specialist supports and facilitates learning and development activities. The role manages and maintains training facilities and resources coordinating event logistics for face-to-face training events providing and/or coordinating on-site and/or remote support

We are currently seeking Sr CRAs with 3 years of monitoring with Oncology experience located in the North Central US. Travel is expected to be nationwide at times target 65% remote visits 4 visits per month 6-8 DOS (including virtual and in person).Job Overview:The Senior CRA I is res

We are currently seeking Sr CRAs with 3 years of monitoring with Oncology experience located in the North Central US. Travel is expected to be nationwide at times target 65% remote visits 4 visits per month 6-8 DOS (including virtual and in person).Job Overview:The Senior CRA I is res

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi